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Sijie
Sijie

... - Oil and sweat glands form an acidic environment which kills many bacteria Other: saliva, sweat, tears, stomach acid kill bacteria, mucus and hair trap pathogens Inflammatory response: - white blood cells leak into infected tissues and destroy pathogens - increase in body temperature (fever), patho ...
C-ImmSim: a model of immunological models - Iac-Cnr
C-ImmSim: a model of immunological models - Iac-Cnr

... Thymus education of T lymphocytes (clonal deletion theory) The clonal Deletion theory, proposed by Burnet, according to which self-reactive lymphoid cells are destroyed during the development of the immune system in an individual. For their work Frank M. Burnet and Peter B. Medawar were awarded the ...
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...  is removed by lymphatics, residual particle are phagocytosed by macrophages Ingrowth of granulation tissue  granulation tissue is highly vascularized connective tissue composed of newly formed capillaries, proliferating fibroblasts and myofibroblasts, cell debris and residual inflammatory cells  ...
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... • Some cytokines may also be associated with the extracellular matrix • Switching between soluble and membrane bound forms of cytokines may be an important immunoregulatory event • Most Cytokines are not stored inside cells (exceptions are, for example TGF-b and PDGF which are stored in platelets) ...
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Microbiology : Unit #2 : Bacteria

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Neutrophil Derived Microvesicles: Emerging Role

... Division of Research, Department of Surgery, University of Cincinnati, Cincinnati, OH, USA Abstract: In response to infection and trauma, exquisite control of the innate inflammatory response is necessary to promote an anti-microbial response and minimize tissue injury. Over the course of the host r ...
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Innate Immunity

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... atherosclerosis was obtained in studies of mice deficient in functional macrophage-colony stimulating factor.4 When such mice were crossed with atherosclerosis-prone apolipoprotein E– deficient (apoE⫺/⫺) mice, the offspring developed little, if any, atherosclerosis. This implies that monocyte differ ...
Development of Mouse Hybridomas by Fusion of Myeloma Cells
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... node lymphocytes produced hybridomas secreting antibodies to the peptide moiety of erythrocyte membrane protein. On the other hand, splenic lymphocyte fusion produced hybridomas secreting antibodies to the carbohydrate moiety of the same antigen.(11) Our data shown here is consistent with the previo ...
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... 1. Endotoxin. Endotoxin is another name for bacterial lipopolysaccharide (LPS) found on all gram negative bacteria. The part of LPS which is responsible for its endotoxin activity is lipid A. LPS is released to a limited extent by growing bacteria, but is released to a large extent upon bacterial ly ...
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... b) Large numbers of mitochondria c) Present mostly during early postnatal life in humans, abundant in hibernating animals for heat production 6. White blood cells (WBCs, leukocytes): These cells enter and leave the blood stream to migrate through, and function in, connective tissues. The most common ...
Triggering receptor expressed on myeloid cells: role in the diagnosis
Triggering receptor expressed on myeloid cells: role in the diagnosis

... increased production of the pro-inflammatory cytokines TNF-a and granulocyte-macrophage colony-stimulating factor, while the production of the anti-inflammatory cytokine IL-10 is reduced. This pattern of activation has suggested a role for this receptor in acute inflammation [8]. Moreover, TREM-1 is ...
Chap 21 The Immune System V10
Chap 21 The Immune System V10

... – Antigen-antibody complexes do not destroy antigens; they prepare them for destruction by innate defenses – Antibodies go after extracellular pathogens; they do not invade solid tissue unless lesion is present • Recent exception found: antibodies can act intracellularly if attached to virus before ...
Cellular immune response induced by Salmonella enterica serotype
Cellular immune response induced by Salmonella enterica serotype

... indicating a Th1 type response, whereas in the later period of the study, increased production of IL-4producing cells suggested a Th2 type response. The results of this study suggest a role for S. Typhi IROMPs in modulating the cellular immune response at peripheral and mucosal levels. ...
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Phagocyte



Phagocytes are cells that protect the body by ingesting (phagocytosing) harmful foreign particles, bacteria, and dead or dying cells. Their name comes from the Greek phagein, ""to eat"" or ""devour"", and ""-cyte"", the suffix in biology denoting ""cell"", from the Greek kutos, ""hollow vessel"". They are essential for fighting infections and for subsequent immunity. Phagocytes are important throughout the animal kingdom and are highly developed within vertebrates. One litre of human blood contains about six billion phagocytes. They were first discovered in 1882 by Ilya Ilyich Mechnikov while he was studying starfish larvae. Mechnikov was awarded the 1908 Nobel Prize in Physiology or Medicine for his discovery. Phagocytes occur in many species; some amoebae behave like macrophage phagocytes, which suggests that phagocytes appeared early in the evolution of life.Phagocytes of humans and other animals are called ""professional"" or ""non-professional"" depending on how effective they are at phagocytosis. The professional phagocytes include many types of white blood cells (such as neutrophils, monocytes, macrophages, mast cells, and dendritic cells). The main difference between professional and non-professional phagocytes is that the professional phagocytes have molecules called receptors on their surfaces that can detect harmful objects, such as bacteria, that are not normally found in the body. Phagocytes are crucial in fighting infections, as well as in maintaining healthy tissues by removing dead and dying cells that have reached the end of their lifespan.During an infection, chemical signals attract phagocytes to places where the pathogen has invaded the body. These chemicals may come from bacteria or from other phagocytes already present. The phagocytes move by a method called chemotaxis. When phagocytes come into contact with bacteria, the receptors on the phagocyte's surface will bind to them. This binding will lead to the engulfing of the bacteria by the phagocyte. Some phagocytes kill the ingested pathogen with oxidants and nitric oxide. After phagocytosis, macrophages and dendritic cells can also participate in antigen presentation, a process in which a phagocyte moves parts of the ingested material back to its surface. This material is then displayed to other cells of the immune system. Some phagocytes then travel to the body's lymph nodes and display the material to white blood cells called lymphocytes. This process is important in building immunity, and many pathogens have evolved methods to evade attacks by phagocytes.
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